Evidence map›Paper›PMID 38697513›Full record

ReviewThe American journal of pathology2024

Finding Your CAR: The Road Ahead for Engineered T Cells.

Po-Han Chen, Rianna Raghunandan, Jon S Morrow, Samuel G Katz

Abstract readReview
In one paragraph

Review in The American journal of pathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Po-Han ChenDepartment of Pathology, Yale School of Medicine, New Haven, Connecticut.
Rianna RaghunandanDepartment of Pathology, Yale School of Medicine, New Haven, Connecticut.
Jon S MorrowDepartment of Pathology, Yale School of Medicine, New Haven, Connecticut.
Samuel G KatzDepartment of Pathology, Yale School of Medicine, New Haven, Connecticut. Electronic address: samuel.katz@yale.edu.

Funding

YALE CANCER CENTER CALABRESI IMMUNO-ONCOLOGY TRAINING PROGRAMK12CA215110 · NCI · YALE UNIVERSITY · PI Harriet M. Kluger · 2018 to 2026
$6.1M
Enhancing Melanoma TIL Efficacy with Multifactor mRNA-Mediated T Cell ReprogrammingR21CA282629 · NCI · YALE UNIVERSITY · PI HURWITZ, MICHAEL E, KATZ, SAMUEL G · 2023 to 2024
$539k
Adoptive Cellular Therapy of T Cell LymphomaR21CA263437 · NCI · YALE UNIVERSITY · PI KATZ, SAMUEL G, LOLIS, ELIAS · 2021 to 2022
$426k
NCI NIH HHS K12 CA215110NCI NIH HHS R21 CA263437NCI NIH HHS R21 CA282629
6 · The paper itself

Abstract

Adoptive cellular therapy using chimeric antigen receptors (CARs) has transformed immunotherapy by engineering T cells to target specific antigens on tumor cells. As the field continues to advance, pathology laboratories will play increasingly essential roles in the complicated multi-step process of CAR T-cell therapy. These include detection of targetable tumor antigens by flow cytometry or immunohistochemistry at the time of disease diagnosis and the isolation and infusion of CAR T cells. Additional roles include: i) detecting antigen loss or heterogeneity that renders resistance to CAR T cells as well as identifying alternative targetable antigens on tumor cells, ii) monitoring the phenotype, persistence, and tumor infiltration properties of CAR T cells and the tumor microenvironment for factors that predict CAR T-cell therapy success, and iii) evaluating side effects and biomarkers of CAR T-cell cytotoxicity such as cytokine release syndrome. This review highlights existing technologies that are applicable to monitoring CAR T-cell persistence, target antigen identification, and loss. Also discussed are emerging technologies that address new challenges such as how to put a brake on CAR T cells. Although pathology laboratories have already provided companion diagnostic tests important in immunotherapy (eg, programmed death-ligand 1, microsatellite instability, and human epidermal growth factor receptor 2 testing), it draws attention to the exciting new translational research opportunities in adoptive cellular therapy.

Indexed as

Immunotherapy, AdoptiveNeoplasmsReceptors, Chimeric AntigenT-LymphocytesAnimalsAntigens, NeoplasmHumansReceptors, Antigen, T-CellTumor MicroenvironmentAntigens, NeoplasmReceptors, Antigen, T-CellReceptors, Chimeric Antigen

Identifiers

PMID38697513
PMCPMC11284763

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.